Rocha B, von Boehmer H, Guy-Grand D
Institut National de la Santé et de la Recherche Médicale, Hôpital Necker-Enfants-Malades, Paris, France.
Proc Natl Acad Sci U S A. 1992 Jun 15;89(12):5336-40. doi: 10.1073/pnas.89.12.5336.
We have studied T-cell receptor (TCR) and alpha/alpha CD8 expression in thymus-independent intraepithelial lymphocytes (TI IELs) from the gut of mice bearing transgenic (TG) TCR alpha beta specific for the male antigen, presented by H-2Db class I major histocompatibility complex (MHC) molecules. In contrast to TCR+ alpha beta cells differentiating in the thymus (from CD4+CD8+ precursors to CD4+CD8- or CD4-CD8+ progeny), TI IELs are not deleted by self-antigens, nor are they positively selected in the absence of the specific peptide. On the contrary, recognition of the antigen in the context of self-MHC is required for selection and granular differentiation of CD8+ TI IELs. Our results also show that, in contrast to the thymus, expression of the beta TG does not block expression of endogenous TCR gamma delta genes in TI IELs. The size of this gut IEL subpopulation and its difference in mechanisms of repertoire selection demonstrate the existence of a major extrathymic pathway of T-cell differentiation, the role of which remains to be elucidated.
我们研究了来自携带对雄性抗原具有特异性的转基因(TG)TCRαβ的小鼠肠道中胸腺非依赖性上皮内淋巴细胞(TI IELs)的T细胞受体(TCR)和α/α CD8表达,该抗原由H-2Db I类主要组织相容性复合体(MHC)分子呈递。与在胸腺中分化的TCR+αβ细胞(从CD4+CD8+前体到CD4+CD8-或CD4-CD8+子代)不同,TI IELs不会被自身抗原清除,在没有特异性肽的情况下也不会被阳性选择。相反,在自身MHC背景下对抗原的识别是CD8+ TI IELs选择和颗粒分化所必需的。我们的结果还表明,与胸腺不同,β TG的表达不会阻断TI IELs中内源性TCRγδ基因的表达。这种肠道IEL亚群的大小及其在谱系选择机制上的差异表明存在一条主要的胸腺外T细胞分化途径,其作用仍有待阐明。